Catálogo de publicaciones - revistas

Compartir en
redes sociales


Science

Resumen/Descripción – provisto por la editorial

No disponible.

Palabras clave – provistas por la editorial

No disponibles.

Disponibilidad
Institución detectada Período Navegá Descargá Solicitá
No detectada desde mar. 1997 / hasta dic. 2023 Science Journals

Información

Tipo de recurso:

revistas

ISSN impreso

0036-8075

ISSN electrónico

1095-9203

Editor responsable

American Association for the Advancement of Science (AAAS)

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

Tabla de contenidos

Governments must halt vulture poisoning

Pablo I. Plaza; Sergio. A. Lambertucci

Palabras clave: Multidisciplinary.

Pp. 1568-1568

Transgender rights rely on inclusive language

Miriam Miyagi; Eartha Mae Guthman; Simón(e) Dow-Kuang Sun

Palabras clave: Multidisciplinary.

Pp. 1568-1569

Brazil’s deception threatens climate goals

Lucas Ferrante; Philip M. Fearnside

Palabras clave: Multidisciplinary.

Pp. 1569-1569

2021 AAAS Kavli Science Journalism Awards announced

Earl Lane; Emily Hughes

<jats:p>Reports from the ongoing pandemic highlighted the entries</jats:p>

Palabras clave: Multidisciplinary.

Pp. 1570-1571

In Science Journals

Michael Funk (eds.)

<jats:p> Highlights from the <jats:italic>Science</jats:italic> family of journals </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1572-1574

In Other Journals

Caroline Ash; Jesse Smith (eds.)

<jats:p>Editors’ selections from the current scientific literature</jats:p>

Palabras clave: Multidisciplinary.

Pp. 1573-1574

Pol IV and RDR2: A two-RNA-polymerase machine that produces double-stranded RNA

Kun HuangORCID; Xiao-Xian WuORCID; Cheng-Li Fang; Zhou-Geng XuORCID; Hong-Wei Zhang; Jian GaoORCID; Chuan-Miao ZhouORCID; Lin-Lin You; Zhan-Xi Gu; Wen-Hui Mu; Yu FengORCID; Jia-Wei WangORCID; Yu ZhangORCID

<jats:title>A tunnel between RNA polymerases</jats:title> <jats:p> Eukaryotes encode five multiple-subunit, DNA-dependent RNA polymerases, of which Pol I, Pol II, and Pol III function as single units to produce cellular single-stranded RNA. The plant-specific Pol IV forms a complex with RDR2 (an RNA-dependent RNA polymerase) to produce double-stranded precursors of small interfering RNA essential for genomic DNA methylation. Huang <jats:italic>et al</jats:italic> . determined the cryo–electron microscopy structures of the Pol IV-RDR2 complex. The structures show that Pol IV and RDR2 connect their active centers through an inner RNA transfer channel and that Pol IV reverses transcription direction and hands over its transcript directly through the channel to RDR2 for the production of the second strand of the double-stranded RNA. —DJ </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1579-1586

An oral SARS-CoV-2 M pro inhibitor clinical candidate for the treatment of COVID-19

Dafydd R. OwenORCID; Charlotte M. N. AllertonORCID; Annaliesa S. Anderson; Lisa Aschenbrenner; Melissa Avery; Simon BerrittORCID; Britton BorasORCID; Rhonda D. Cardin; Anthony Carlo; Karen J. CoffmanORCID; Alyssa Dantonio; Li DiORCID; Heather EngORCID; RoseAnn FerreORCID; Ketan S. Gajiwala; Scott A. Gibson; Samantha E. GreasleyORCID; Brett L. HurstORCID; Eugene P. KadarORCID; Amit S. KalgutkarORCID; Jack C. Lee; Jisun LeeORCID; Wei Liu; Stephen W. Mason; Stephen NoellORCID; Jonathan J. NovakORCID; R. Scott ObachORCID; Kevin Ogilvie; Nandini C. PatelORCID; Martin PetterssonORCID; Devendra K. Rai; Matthew R. ReeseORCID; Matthew F. SammonsORCID; Jean G. Sathish; Ravi Shankar P. SinghORCID; Claire M. SteppanORCID; Al E. Stewart; Jamison B. Tuttle; Lawrence Updyke; Patrick R. Verhoest; Liuqing Wei; Qingyi Yang; Yuao Zhu

<jats:title>Path to another drug against COVID-19</jats:title> <jats:p> The rapid development of vaccines has been crucial in battling the ongoing COVID-19 pandemic. However, access challenges remain, breakthrough infections occur, and emerging variants present increased risk. Developing antiviral therapeutics is therefore a high priority for the treatment of COVID-19. Some drug candidates in clinical trials act against the viral RNA-dependent RNA polymerase, but there are other viral enzymes that have been considered good targets for inhibition by drugs. Owen <jats:italic>et al</jats:italic> . report the discovery and characterization of a drug against the main protease involved in the cleavage of polyproteins involved in viral replication. The drug, PF-07321332, can be administered orally, has good selectivity and safety profiles, and protects against infection in a mouse model. In a phase 1 clinical trial, the drug reached concentrations expected to inhibit the virus based on in vitro studies. It also inhibited other coronaviruses, including severe acute respiratory syndrome coronavirus 1 and Middle East respiratory syndrome coronavirus, and could be in the armory against future viral threats. —VV </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1586-1593

Enhancement of lithium-mediated ammonia synthesis by addition of oxygen

Katja LiORCID; Suzanne Z. AndersenORCID; Michael J. StattORCID; Mattia SaccoccioORCID; Vanessa J. BukasORCID; Kevin KremplORCID; Rokas SažinasORCID; Jakob B. PedersenORCID; Vahid ShadravanORCID; Yuanyuan ZhouORCID; Debasish ChakrabortyORCID; Jakob KibsgaardORCID; Peter C. K. VesborgORCID; Jens K. NørskovORCID; Ib ChorkendorffORCID

<jats:title>Boosting ammonia with a little oxygen</jats:title> <jats:p> Ammonia synthesis from nitrogen for fertilizer production is highly energy intensive. Chemists are therefore exploring electrochemical approaches that could draw power from renewable sources while generating less waste. One promising cycle involves the reduction of lithium ions at an electrode, with the resultant metal in turn reducing nitrogen and regenerating the ions. Li <jats:italic>et al</jats:italic> . report the counterintuitive result that small quantities of oxygen could enhance the efficiency of this process, which they attribute to diffusional effects that limit excessive lithium reduction. —JSY </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1593-1597

Stabilized tilted-octahedra halide perovskites inhibit local formation of performance-limiting phases

Tiarnan A. S. DohertyORCID; Satyawan NaganeORCID; Dominik J. KubickiORCID; Young-Kwang JungORCID; Duncan N. JohnstoneORCID; Affan N. IqbalORCID; Dengyang GuoORCID; Kyle FrohnaORCID; Mohsen DanaieORCID; Elizabeth M. TennysonORCID; Stuart MacphersonORCID; Anna AbfaltererORCID; Miguel AnayaORCID; Yu-Hsien ChiangORCID; Phillip CroutORCID; Francesco Simone RuggeriORCID; Sean CollinsORCID; Clare P. GreyORCID; Aron WalshORCID; Paul A. MidgleyORCID; Samuel D. StranksORCID

<jats:title>Stable but not quite cubic</jats:title> <jats:p> The black, photoactive phase of formamidinium (FA) perovskites, which is usually stabilized by cation alloying to avoid the formation of inactive hexagonal phases, is assumed to be cubic. High-resolution microscopy studies by Doherty <jats:italic>et al</jats:italic> . using nanoscale probes revealed that these FA-rich phases are not cubic but rather undergo slight tilting (by two degrees) of the octahedra. Black phases can have localized regions of hexagonal phases that nucleate degradation. Surface-bound ethylenediaminetetraacetic acid stabilized the tilted phase of pure FA lead triiodide against environmental degradation. —PDS </jats:p>

Palabras clave: Multidisciplinary.

Pp. 1598-1605